Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q238
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.509 |
CLV_Separin_Metazoa | 175 | 179 | PF03568 | 0.479 |
DEG_SPOP_SBC_1 | 63 | 67 | PF00917 | 0.816 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.522 |
DOC_MAPK_DCC_7 | 326 | 335 | PF00069 | 0.608 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.608 |
DOC_MIT_MIM_1 | 261 | 270 | PF04212 | 0.568 |
DOC_SPAK_OSR1_1 | 8 | 12 | PF12202 | 0.633 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.708 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.826 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 108 | 116 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 120 | 126 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 316 | 325 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 339 | 347 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 439 | 446 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.608 |
LIG_Actin_WH2_2 | 233 | 250 | PF00022 | 0.553 |
LIG_AP2alpha_2 | 432 | 434 | PF02296 | 0.612 |
LIG_CtBP_PxDLS_1 | 303 | 307 | PF00389 | 0.555 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.636 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.385 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.625 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.628 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.684 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.510 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.525 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.644 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.580 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.592 |
LIG_Integrin_isoDGR_2 | 435 | 437 | PF01839 | 0.637 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 232 | 242 | PF02991 | 0.669 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.599 |
LIG_PTB_Apo_2 | 3 | 10 | PF02174 | 0.514 |
LIG_Rb_LxCxE_1 | 245 | 262 | PF01857 | 0.619 |
LIG_RPA_C_Fungi | 388 | 400 | PF08784 | 0.567 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.630 |
LIG_SH3_1 | 344 | 350 | PF00018 | 0.595 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.708 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.712 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.683 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.530 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.609 |
LIG_SUMO_SIM_anti_2 | 172 | 180 | PF11976 | 0.531 |
LIG_SUMO_SIM_anti_2 | 24 | 30 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 20 | 27 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 302 | 307 | PF11976 | 0.551 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.629 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.661 |
LIG_TRAF2_1 | 413 | 416 | PF00917 | 0.575 |
LIG_TYR_ITIM | 92 | 97 | PF00017 | 0.616 |
MOD_CDK_SPK_2 | 321 | 326 | PF00069 | 0.803 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.542 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.536 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.623 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.294 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.701 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.709 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.477 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.527 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.642 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.703 |
MOD_DYRK1A_RPxSP_1 | 321 | 325 | PF00069 | 0.733 |
MOD_DYRK1A_RPxSP_1 | 346 | 350 | PF00069 | 0.590 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.530 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.538 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.695 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.819 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.553 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.731 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.627 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.612 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.601 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.808 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.583 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.626 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.741 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.648 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.804 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.534 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.531 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.468 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.519 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.521 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.691 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.803 |
MOD_OFUCOSY | 13 | 18 | PF10250 | 0.504 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.544 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.564 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.802 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.751 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.648 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.521 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.772 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.631 |
MOD_PKB_1 | 437 | 445 | PF00069 | 0.524 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.536 |
MOD_Plk_2-3 | 259 | 265 | PF00069 | 0.591 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.542 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.447 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.508 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.536 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.604 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.706 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.791 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.828 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.523 |
MOD_SUMO_for_1 | 39 | 42 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 127 | 132 | PF00179 | 0.643 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.619 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.668 |
TRG_Pf-PMV_PEXEL_1 | 439 | 444 | PF00026 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0I6 | Leptomonas seymouri | 57% | 94% |
A0A3S5H814 | Leishmania donovani | 91% | 100% |
A4HNP8 | Leishmania braziliensis | 78% | 100% |
A4ICU7 | Leishmania infantum | 91% | 100% |
E9ASF7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |